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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288655Generated: November 4, 2026

2,6-Lutidine → HCID 54382601, compound

https://huagongshe.com/reaction/1288655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantButyl iodideHCID 10962—
ReactantHCID 54158792HCID 54158792—
ProductHCID 54382601HCID 54382601—

Reaction Conditions

Temperature135 °C

Reaction Steps

N-(4-Chlorophenyl)alanine ethyl ester (4.5 g, 0.02 mol), n-butyl iodide (3.6 g, 0.02 mol) and 2,6-lutidine (2.5 g, 0.025 mol) were sealed in a glass tube and the contents were heated at 135° C. for 48 h. The tube was then cooled, and the contents were partitioned between 250 mL ethyl acetate and 200 mL brine. The organic layer was separated, dried over anhyd. sodium sulfate, and concentrated at reduced pressure. The resulting oil was chromatographed on silica gel using heptane:THF (4:1) as the eluant. The ester was isolated as a colorless oil (2.5 g, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747236
Source datasetuspto-grants-1998_05
ORD IDord-8811b95d01a945618ba291218b48357b
Source noteuspto-grants-1998_05